Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.46 (A)
Location

Chromosome 11:69809515 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74235985

HGVS name

11:g.69809515A>C

About this variant

This variant overlaps 1 transcript and has 2522 individual genotypes.

Variation displays